Dexamethasone
- Product NDC
- 50090-0088
- 11-digit product format
- 500900088
- Labeler code
- 50090
- Product ID
- 50090-0088_5cffc27e-187b-487a-bba0-5a18da78abfa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA084612
- Marketing category
- ANDA
- Marketing start
- 1978-07-19
- Marketing end
- 0000-00-00
- Substance
- DEXAMETHASONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0088-0 | 50090008800 | 30 TABLET in 1 BOTTLE (50090-0088-0) | 30 tablet | 2018-10-23 | 0000-00-00 | No | No | Current |
| 50090-0088-4 | 50090008804 | 6 TABLET in 1 BOTTLE, PLASTIC (50090-0088-4) | 6 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |